HK1136820A1 - Substituted arylimidazolone and triazolone as inhibitors of vasopressin receptors - Google Patents

Substituted arylimidazolone and triazolone as inhibitors of vasopressin receptors

Info

Publication number
HK1136820A1
HK1136820A1 HK10100511.8A HK10100511A HK1136820A1 HK 1136820 A1 HK1136820 A1 HK 1136820A1 HK 10100511 A HK10100511 A HK 10100511A HK 1136820 A1 HK1136820 A1 HK 1136820A1
Authority
HK
Hong Kong
Prior art keywords
arylimidazolone
triazolone
inhibitors
substituted
vasopressin receptors
Prior art date
Application number
HK10100511.8A
Other languages
Chinese (zh)
Inventor
Heinrich Meier
Eckhard Bender
Ulf Brggemeier
Ingo Flamme
Dagmar Karthaus
Peter Kolkhof
Daniel Meibom
Dirk Schneider
Verena Voehringer
Chantal Frstner
Jrg Keldenich
Dieter Lang
Elisabeth Pook
Carsten Schmeck
Original Assignee
Bayer Ip Gmbh
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Bayer Ip Gmbh filed Critical Bayer Ip Gmbh
Publication of HK1136820A1 publication Critical patent/HK1136820A1/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D249/12—Oxygen or sulfur atoms
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4164—1,3-Diazoles
    • A61K31/4166—1,3-Diazoles having oxo groups directly attached to the heterocyclic ring, e.g. phenytoin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/12—Drugs for disorders of the metabolism for electrolyte homeostasis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A61P7/10—Antioedematous agents; Diuretics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D233/70—One oxygen atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
HK10100511.8A 2006-05-23 2010-01-18 Substituted arylimidazolone and triazolone as inhibitors of vasopressin receptors HK1136820A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102006024024A DE102006024024A1 (en) 2006-05-23 2006-05-23 Substituted arylimidazolones and triazolones and their use
PCT/EP2007/004615 WO2007134862A1 (en) 2006-05-23 2007-05-21 Substituted arylimidaz0l0ne and triaz0l0ne as inhibitors of vasopressin receptors

Publications (1)

Publication Number Publication Date
HK1136820A1 true HK1136820A1 (en) 2010-07-09

Family

ID=38353593

Family Applications (1)

Application Number Title Priority Date Filing Date
HK10100511.8A HK1136820A1 (en) 2006-05-23 2010-01-18 Substituted arylimidazolone and triazolone as inhibitors of vasopressin receptors

Country Status (30)

Country Link
US (2) US8084481B2 (en)
EP (1) EP2027096B8 (en)
JP (1) JP5247684B2 (en)
KR (1) KR101426574B1 (en)
CN (1) CN101495458B (en)
AR (1) AR061114A1 (en)
AU (1) AU2007253572B9 (en)
BR (1) BRPI0711975A2 (en)
CA (1) CA2652834C (en)
DE (1) DE102006024024A1 (en)
DK (1) DK2027096T3 (en)
DO (1) DOP2007000102A (en)
EC (1) ECSP088904A (en)
ES (1) ES2385606T3 (en)
GT (1) GT200800250A (en)
HK (1) HK1136820A1 (en)
HN (1) HN2008001720A (en)
IL (1) IL195142A (en)
MA (1) MA30500B1 (en)
MX (1) MX2008014797A (en)
PE (1) PE20080706A1 (en)
PL (1) PL2027096T3 (en)
PT (1) PT2027096E (en)
RU (1) RU2460724C2 (en)
SV (1) SV2009003098A (en)
TN (1) TNSN08443A1 (en)
TW (1) TW200817336A (en)
UY (1) UY30364A1 (en)
WO (1) WO2007134862A1 (en)
ZA (1) ZA200809860B (en)

Families Citing this family (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102006024024A1 (en) * 2006-05-23 2007-11-29 Bayer Healthcare Aktiengesellschaft Substituted arylimidazolones and triazolones and their use
MX2011003780A (en) * 2008-10-10 2011-05-03 Janssen Pharmaceutica Nv Combination therapy comprising angiotensin receptor blockers and vasopressin receptor antagonists.
DE102008060967A1 (en) 2008-12-06 2010-06-10 Bayer Schering Pharma Aktiengesellschaft Substituted phenylsulfonyltriazolones and their use
DE102010001064A1 (en) * 2009-03-18 2010-09-23 Bayer Schering Pharma Aktiengesellschaft Substituted 2-acetamido-5-aryl-1,2,4-triazolones and their use
DE102009013642A1 (en) * 2009-03-18 2010-09-23 Bayer Schering Pharma Aktiengesellschaft Substituted phenylalanine derivatives and their use
DE102009028929A1 (en) * 2009-08-27 2011-07-07 Bayer Schering Pharma Aktiengesellschaft, 13353 Heterocyclic-substituted 2-acetamido-5-aryl-1,2,4-triazolones and their use
DK2539326T3 (en) 2010-02-27 2017-08-28 Bayer Ip Gmbh BIS-ARYL-CONNECTED ARYLTRIZOLONES AND USE THEREOF
EP2995317A1 (en) 2010-05-26 2016-03-16 Satiogen Pharmaceuticals, Inc. Bile acid recycling inhibitors and satiogens for treatment of diabetes, obesity, and inflammatory gastrointestinal conditions
DE102010040187A1 (en) * 2010-09-02 2012-03-08 Bayer Schering Pharma Aktiengesellschaft Substituted N-phenethyl-triazolone acetamides and their use
DE102010040924A1 (en) * 2010-09-16 2012-03-22 Bayer Schering Pharma Aktiengesellschaft Substituted phenylacet and phenylpropanamides and their use
WO2012043791A1 (en) 2010-10-01 2012-04-05 大正製薬株式会社 1,2,4-triazolone derivative
CN102260154A (en) * 2011-06-10 2011-11-30 南通职业大学 Preparation method of pharmaceutical intermediate alpha-bromo-p-chloropropiophenone
CN102875499B (en) * 2011-07-12 2015-08-19 天津药明康德新药开发有限公司 The preparation method of 3-aminomethyl trimethylene oxide and organic acid salt thereof
EP4234545A3 (en) * 2011-07-29 2023-09-06 Karyopharm Therapeutics Inc. Hydrazide containing nuclear transport modulators and uses thereof
CA2853227C (en) * 2011-10-27 2019-05-14 Taisho Pharmaceutical Co., Ltd. Azole derivative
EA030839B1 (en) 2011-10-28 2018-10-31 ЛУМЕНА ФАРМАСЬЮТИКАЛС ЭлЭлСи Bile acid recycling inhibitors for treatment of pediatric cholestatic liver diseases
KR20210131431A (en) 2011-10-28 2021-11-02 샤이어 휴먼 지네틱 테라피즈 인크. Bile acid recycling inhibitors for treatment of hypercholemia and cholestatic liver disease
CN105228615A (en) 2013-03-15 2016-01-06 鲁美纳医药公司 Be used for the treatment of the bile acid recycling inhibitors of Barrett esophagus and gastroesophageal reflux disease
AU2014228850A1 (en) 2013-03-15 2015-10-29 Lumena Pharmaceuticals Llc Bile acid recycling inhibitors for treatment of primary sclerosing cholangitis and inflammatory bowel disease
JP6387669B2 (en) * 2013-04-26 2018-09-12 大正製薬株式会社 Medicaments containing azole derivatives
US10392381B2 (en) * 2014-07-18 2019-08-27 Ohio University Prevention and treatment of non-alcoholic fatty liver disease
MY186908A (en) 2014-11-03 2021-08-26 Bayer Pharma AG Hydroxyalkyl-substituted phenyltriazole derivatives and uses thereof
GB201504763D0 (en) * 2015-03-20 2015-05-06 Mironid Ltd Compounds and uses
WO2017191115A1 (en) * 2016-05-03 2017-11-09 Bayer Pharma Aktiengesellschaft Oxoalkyl-substituted phenyltriazole derivatives and uses thereof
US9988367B2 (en) 2016-05-03 2018-06-05 Bayer Pharma Aktiengesellschaft Amide-substituted pyridinyltriazole derivatives and uses thereof
WO2017191117A1 (en) 2016-05-03 2017-11-09 Bayer Pharma Aktiengesellschaft V1a receptor antagonists for use in the treatment of renal diseases
US20200337590A1 (en) 2018-01-16 2020-10-29 Bayer Aktiengesellschaft Assistance in the treatment of cardiac insufficiency
WO2020167958A1 (en) 2019-02-12 2020-08-20 Mirum Pharmaceuticals, Inc. Methods for treating cholestasis
WO2021127459A1 (en) * 2019-12-20 2021-06-24 Blackthorn Therapeutics, Inc. Gpr139 receptor modulators
WO2023041422A1 (en) 2021-09-20 2023-03-23 Basf Se Heterocyclic compounds for the control of invertebrate pests

Family Cites Families (39)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3042466A1 (en) 1980-11-11 1982-06-16 A. Nattermann & Cie GmbH, 5000 Köln N-SUBSTITUTED (OMEGA) - (2-OXO-4-IMIDAZOLIN-L-YL) -ALKANIC ACID DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF AND PHARMACEUTICAL PREPARATIONS CONTAINING THEM
EP0412594B1 (en) 1989-07-28 1996-01-03 Merck & Co. Inc. Substituted triazolinones, triazolinethiones, and triazolinimines as angiotensin II antagonists
US5468448A (en) 1989-12-28 1995-11-21 Ciba-Geigy Corporation Peroxide disinfection method and devices therefor
DE4107857A1 (en) 1991-03-12 1992-09-17 Thomae Gmbh Dr K CYCLIC UREA DERIVATIVES, MEDICAMENTS CONTAINING SUCH COMPOUNDS AND METHOD FOR THE PRODUCTION THEREOF
IT1251488B (en) 1991-09-17 1995-05-15 Mini Ricerca Scient Tecnolog OSSA (TIA) DIAZOL- AND TRIAZOL-ONI (TIONI) WITH ACARICIDE AND INSECTICIDE ACTIVITY
RU2116304C1 (en) * 1992-04-28 1998-07-27 Такеда Кемикал Индастриз, Лтд. Derivatives of azole, method of their synthesis, pharmaceutical composition
SK94393A3 (en) 1992-09-11 1994-08-10 Thomae Gmbh Dr K Cyclic derivatives of urea, process for their production and their pharmaceutical agents with the content of those
US6844005B2 (en) 2002-02-25 2005-01-18 Trutek Corp Electrostatically charged nasal application product with increased strength
FR2708608B1 (en) 1993-07-30 1995-10-27 Sanofi Sa N-sulfonylbenzimidazolone derivatives, their preparation, pharmaceutical compositions containing them.
US5897858A (en) 1994-02-03 1999-04-27 Schering-Plough Healthcare Products, Inc. Nasal spray compositions exhibiting increased retention in the nasal cavity
TW467902B (en) * 1996-07-31 2001-12-11 Bristol Myers Squibb Co Diphenyl heterocycles as potassium channel modulators
DE19741235A1 (en) * 1997-09-18 1999-03-25 Hoechst Marion Roussel De Gmbh Novel imidazolidine derivatives, their preparation, their use and pharmaceutical compositions containing them
ES2243016T3 (en) 1997-12-17 2005-11-16 MERCK & CO., INC. INTEGRINE RECEIVER ANTAGONISTS.
DE19816882A1 (en) 1998-04-17 1999-10-21 Boehringer Ingelheim Pharma Use of known and new triazolone derivatives as medicaments, especially for treatment of neurodegenerative disorders and cerebral ischemia
DE19914140A1 (en) 1999-03-27 2000-09-28 Bayer Ag Substituted benzoylpyrazoles
DE19920791A1 (en) 1999-05-06 2000-11-09 Bayer Ag Substituted benzoyl isoxazoles
DE19921424A1 (en) 1999-05-08 2000-11-09 Bayer Ag Substituted benzoyl ketones
DE19929348A1 (en) 1999-06-26 2000-12-28 Bayer Ag Pure 2-heterocyclylmethyl-benzoic acid derivative preparation in high yield, for use as pharmaceutical or agrochemical intermediate, from phthalide compound and nitrogen-containing heterocycle
US6531142B1 (en) 1999-08-18 2003-03-11 The Procter & Gamble Company Stable, electrostatically sprayable topical compositions
DE19943635A1 (en) 1999-09-13 2001-03-15 Bayer Ag Novel aminodicarboxylic acid derivatives with pharmaceutical properties
DE19943636A1 (en) 1999-09-13 2001-03-15 Bayer Ag Novel dicarboxylic acid derivatives with pharmaceutical properties
DE19943639A1 (en) 1999-09-13 2001-03-15 Bayer Ag Dicarboxylic acid derivatives with novel pharmaceutical properties
DE19943634A1 (en) 1999-09-13 2001-04-12 Bayer Ag Novel dicarboxylic acid derivatives with pharmaceutical properties
WO2002066447A1 (en) 2001-02-21 2002-08-29 Ono Pharmaceutical Co., Ltd. 4h-1,2,4-triazole-3(2h)-thione deratives as sphingomyelinase inhibitors
DE10110750A1 (en) 2001-03-07 2002-09-12 Bayer Ag Novel aminodicarboxylic acid derivatives with pharmaceutical properties
DE10110749A1 (en) 2001-03-07 2002-09-12 Bayer Ag Substituted aminodicarboxylic acid derivatives
US20040071757A1 (en) 2001-11-20 2004-04-15 David Rolf Inhalation antiviral patch
JP4673295B2 (en) * 2003-03-14 2011-04-20 メルク・シャープ・エンド・ドーム・コーポレイション Monocyclic anilide spirohydantoin CGRP receptor antagonist
CA2571907A1 (en) 2003-06-27 2005-01-27 Berglin Corporation Of Washington Machine for precision low stress coring and slicing of apples and other soft-cored or pitted fruits
CA2532089C (en) 2003-07-16 2012-05-22 Duramed Pharmaceuticals, Inc. Methods of hormonal treatment utilizing contraceptive regimens with continuous estrogen administration
EP1722784A4 (en) 2004-03-08 2009-08-12 Wyeth Corp Ion channel modulators
JP2007527911A (en) 2004-03-08 2007-10-04 ワイス Ion channel modulator
JP2007527909A (en) 2004-03-08 2007-10-04 ワイス Ion channel modulator
EP1742932A1 (en) * 2004-04-28 2007-01-17 Pfizer Limited 3-heterocyclyl-4-phenyl-triazole derivatives as inhibitors of the vasopressin v1a receptor
US7642275B2 (en) 2004-12-16 2010-01-05 Takeda San Diego, Inc. Histone deacetylase inhibitors
WO2006117657A1 (en) 2005-05-03 2006-11-09 Ranbaxy Laboratories Limited Triazolone derivatives as anti-inflammatory agents
DE102006024024A1 (en) * 2006-05-23 2007-11-29 Bayer Healthcare Aktiengesellschaft Substituted arylimidazolones and triazolones and their use
WO2008052031A2 (en) 2006-10-24 2008-05-02 Alcon Research, Ltd. 2-pyrrolidone derivatives for preservation of ophthalmic, otic and nasal compositions
DE102010001064A1 (en) * 2009-03-18 2010-09-23 Bayer Schering Pharma Aktiengesellschaft Substituted 2-acetamido-5-aryl-1,2,4-triazolones and their use

Also Published As

Publication number Publication date
KR101426574B1 (en) 2014-08-06
HN2008001720A (en) 2009-06-10
JP2009537581A (en) 2009-10-29
RU2460724C2 (en) 2012-09-10
MA30500B1 (en) 2009-06-01
CN101495458B (en) 2014-01-29
PE20080706A1 (en) 2008-08-07
AU2007253572B9 (en) 2013-07-25
US20090312381A1 (en) 2009-12-17
BRPI0711975A2 (en) 2012-02-22
GT200800250A (en) 2009-09-14
ECSP088904A (en) 2008-12-30
MX2008014797A (en) 2008-12-02
SV2009003098A (en) 2009-04-28
PT2027096E (en) 2012-07-12
US8084481B2 (en) 2011-12-27
EP2027096B8 (en) 2012-09-26
CA2652834C (en) 2015-01-27
IL195142A (en) 2013-07-31
TW200817336A (en) 2008-04-16
TNSN08443A1 (en) 2010-04-14
AU2007253572A1 (en) 2007-11-29
CN101495458A (en) 2009-07-29
EP2027096B1 (en) 2012-05-23
PL2027096T3 (en) 2012-10-31
ES2385606T3 (en) 2012-07-27
US20130005704A1 (en) 2013-01-03
IL195142A0 (en) 2009-09-22
WO2007134862A1 (en) 2007-11-29
CA2652834A1 (en) 2007-11-29
DE102006024024A1 (en) 2007-11-29
UY30364A1 (en) 2008-01-02
KR20090014214A (en) 2009-02-06
DOP2007000102A (en) 2007-12-31
EP2027096A1 (en) 2009-02-25
AU2007253572B2 (en) 2013-06-20
AR061114A1 (en) 2008-08-06
ZA200809860B (en) 2010-02-24
ES2385606T8 (en) 2013-05-14
JP5247684B2 (en) 2013-07-24
RU2008150598A (en) 2010-06-27
DK2027096T3 (en) 2012-09-10

Similar Documents

Publication Publication Date Title
HK1136820A1 (en) Substituted arylimidazolone and triazolone as inhibitors of vasopressin receptors
GB0622084D0 (en) Inhibitors of HSP90
EP2026843A4 (en) Therapeutic uses of inhibitors of rtp801l
ZA200802585B (en) Pyridopyrimidinone inhibitors of Pl3Kα
IL190292A0 (en) PYRIDOPYRIMIDINONE INHIBITORS OF P13Ka
ZA200808282B (en) Uses of DPP-IV inhibitors
IL193587A0 (en) Heterobicyclic pyrazole compounds and methods of use
ZA200906946B (en) Inhibitors of iap
EP2192838A4 (en) Heterocyclic inhibitors of necroptosis
PL2040728T3 (en) Fkbp-l and uses thereof as inhibitors of angiogenesis
IL197869A0 (en) Compositions of chk1 inhibitors
IL193482A0 (en) Hydantoin based kinase inhibitors
EP2054056A4 (en) Small molecule inhibitors of kynurenine-3-monooxygenase
EP2084139A4 (en) Oxazolidinium compounds and use as hydrate inhibitors
EP1973915A4 (en) Triazole derivatives as inhibitors of 11-beta-hydroxysteroid dehydrogenase-1
EP2054397A4 (en) Small molecule inhibitors of kynurenine-3-monooxygenase
HK1137756A1 (en) Substituted dihydropyrazolones and use thereof as hif-prolyl-4 -hydroxylase inhibitors hif--4-
IL198471A0 (en) Substituted pyrazole and triazole compounds as ksp inhibitors
EP2046827A4 (en) Mimotope receptors and inhibitors for platelet- platelet and platelet-endothelium interactions
GB0808286D0 (en) Inhibitors of HSP90
GB0622085D0 (en) Inhibitors of HSP90
IL198149A0 (en) Novel inhibitors of chymase
ZA200806993B (en) Hydantoin based kinase inhibitors
GB0608822D0 (en) Inhibitors of DHFR
SI2035379T1 (en) Inhibitors of 11-beta-hydroxysteroid dehydrogenase 1

Legal Events

Date Code Title Description
PC Patent ceased (i.e. patent has lapsed due to the failure to pay the renewal fee)

Effective date: 20180521